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Dive into the research topics where Mohammed F Qutub is active.

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Featured researches published by Mohammed F Qutub.


British Journal of Ophthalmology | 2015

Sebaceous adenomas of the eyelid and Muir-Torre Syndrome

Lisa Jagan; Pablo Zoroquiain; Vasco Bravo-Filho; Patrick Logan; Mohammed F Qutub; Miguel N. Burnier

Background/aims Sebaceous adenomas (SAs) are rare, benign sebaceous gland tumours of the eyelid. SAs may be associated with primary internal malignancies. This association is known as Muir-Torre Syndrome (MTS). The purpose of this study was to approximate the prevalence of SAs, to determine the reliability of the clinical diagnosis of SAs and to demonstrate immunohistochemical staining of DNA mismatch repair proteins mutL homologue 1 (MLH1) and mutS homologue 2 (MSH2) for a case of MTS. Methods We reviewed the histopathology reports from all eyelid specimens collected between 1993 and 2013 at the Henry C Witelson Ocular Pathology Laboratory to determine the proportion of SAs. For the SAs identified on histopathology, we looked at patient charts to see what diagnosis was originally suspected on clinical examination. Immunohistochemical staining for MLH1 and MSH2 was performed on all SAs to screen for MTS. Results Of the 5884 eyelid specimens collected, 9 were SAs (6 women, 3 men; 42–72 years old). The diagnosis of SA was suspected clinically in only one of the nine cases based on the gross appearance of the eyelid lesion. Immunohistochemistry revealed one SA case with positive MLH1 expression and negative MSH2 expression. These findings prompted systemic work-up and this patient was diagnosed with MTS after discovery of a colon adenocarcinoma T2M0N0. Conclusions The diagnosis of eyelid SA is rare. The importance of this benign eyelid tumour stems from its association with internal malignancies in MTS. Immunohistochemical staining of mismatch repair proteins MLH1 and MSH2 is a valid and accessible strategy for investigating MTS in patients with SAs.


Journal of Medical Case Reports | 2014

Superficial epithelioma with sebaceous differentiation involving the eyelid: a case report

Sultan Aldrees; Pablo Zoroquiain; Patrick Logan; Mohammed F Qutub; Natalia Vila; Vasco Bravo-Filho; Conrad Kavalec; Miguel N. Burnier

IntroductionSuperficial epithelioma with sebaceous differentiation is a rare benign epithelial neoplasm. It usually involves the head, neck or the back of a middle-age person. To the best of our knowledge, two ocular cases have been reported in the literature.Case presentationA 46-year-old man of Italian descent, with a known history of testicular seminoma treated by orchiectomy with chemotherapy and radiotherapy, presented with a tan-colored lesion measuring 4mm in diameter in his right upper lid that had been growing over 10 months. It was clinically diagnosed as papilloma. An excisional biopsy was done. On histological examination, the lesion was a well-circumscribed and sharply demarcated epithelial tumor attached to the overlying epidermis and characterized by plate-like proliferation of basaloid to squamous cells with clusters of mature sebaceous cells and foci of ductal differentiation. After a follow-up period of 5 months, no recurrence of the lesion has been documented.ConclusionsSuperficial epithelioma with sebaceous differentiation is part of the differential diagnoses of eyelid lesions. Arguments in the literature about the correct nomenclature of superficial epithelioma with sebaceous differentiation have resulted in under-diagnosed cases. The benign histological features and the lack of recurrence support its benign nature. Although no clear association has linked superficial epithelioma with sebaceous differentiation with Muir–Torre syndrome, further clinical correlation and close follow up for patients are recommended.


International Journal of Ophthalmic Pathology | 2016

Toll-Like Receptor 3 is Expressed in All Layers of the Human Sensory Retina and Retinal Pigment Epithelium

Mohammed F Qutub; Pablo Zoroquiain; Shawn C. Maloney; Sultan Aldrees; Miguel Jr Burnier


Investigative Ophthalmology & Visual Science | 2015

Evaluating the in vivo efficacy of a novel first in class drug for the treatment of primary uveal melanoma

Patrick Logan; Sultan Aldrees; Mohammed F Qutub; Natalia Vila; Vasco Bravo-Filho; Miguel N. Burnier


Investigative Ophthalmology & Visual Science | 2015

Programmed cell death ligand 1 is highly expressed in uveal melanoma

Pablo Zoroquiain; Dominique Fausto de Souza; Joao Mansure; Mohammed F Qutub; Juliana Portela Passos


Investigative Ophthalmology & Visual Science | 2015

The effects of acetylsalicylic acid as an anti-tumor agent in a metastatic ocular melanoma cell line

Dominique Fausto de Souza; Sultan Aldrees; Mohammed F Qutub; Sarah Alghamdi; Ana Beatriz Toledo Dias; Miguel N. Burnier


Investigative Ophthalmology & Visual Science | 2015

A large series of blind painful eyes: potential causes and associated histopathological features

Cristina Fonseca; Norah Alsaif; Mohammed F Qutub; S. Bakalian; Vasco Bravo-Filho; Miguel N. Burnier


Investigative Ophthalmology & Visual Science | 2015

The Importance of Sox-10 Expression in Uveal Melanoma

Sarah Alghamdi; Ana Beatriz Toledo Dias; Mohammed F Qutub; Julia Caminal; Josep M. Marti; Miguel N. Burnier


Investigative Ophthalmology & Visual Science | 2015

Pericyte loss in vitrectomy samples is a sensitive and specific marker of diabetic retinopathy

Mohammed F Qutub; Sultan Aldrees; Natalia Vila; Michael A. Kapusta; John C. Chen; Miguel N. Burnier


Investigative Ophthalmology & Visual Science | 2015

Gonadotropin releasing hormone receptor is expressed in retinoblastomas and a retinoblastoma cell line

Sultan Aldrees; Pablo Zoroquiain; Mohammed F Qutub; Sarah Alghamdi; Taylor Nayman; Miguel N. Burnier

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